What is the use of 2/3 Diphenylquinoxaline?
Use: Used as anti-viral, anti-bacterial, anti-inflammatory, anti-protozoal, anti-cancer (colon cancer therapies), antidepressant, anti-HIV agent and as kinase inhibitor etc.
What is the Iupac name of 2/3 Diphenylquinoxaline?
2,3-Diphenylquinoxaline
| PubChem CID | 74311 |
|---|---|
| Structure | Find Similar Structures |
| Chemical Safety | Laboratory Chemical Safety Summary (LCSS) Datasheet |
| Molecular Formula | C20H14N2 |
| Synonyms | 2,3-Diphenylquinoxaline 1684-14-6 QUINOXALINE, 2,3-DIPHENYL- 2,3-Diphenyl-quinoxaline UNII-5MJ74FC4Q6 More… |
What is the molecular weight of 2/3 Diphenylquinoxaline?
282.3
2,3-Diphenylquinoxaline
| PubChem CID | 74311 |
|---|---|
| Chemical Safety | Laboratory Chemical Safety Summary (LCSS) Datasheet |
| Molecular Formula | C20H14N2 |
| Synonyms | 2,3-Diphenylquinoxaline 1684-14-6 QUINOXALINE, 2,3-DIPHENYL- 2,3-Diphenyl-quinoxaline UNII-5MJ74FC4Q6 More… |
| Molecular Weight | 282.3 |
What is the melting point of 2/3 Diphenylquinoxaline?
125-127 °C
mp. 125-127 °C (lit.)
Which reaction is involved in synthesis of 2/3 diphenyl quinoxaline?
Principle: This is a method of condensation of an aryl 1,2-diamine with a 1,2-dicarbonyl compound by heating in a solvent like rectified sprit. Here condensation reaction of 1,2-diamines with α-diketones occurs with cyclization. Aim: To prepare 2,3- diphenylquinoxaline from benzyl.
Which of the following vitamins contain pteridine ring *?
Folic acid consists of three moieties: the pterin (or pteridine) ring, which is conjugated to PABA by a methylene bridge, which is in turn joined to a glutamic residue via a peptide bond. Folic acid is the fully oxidized monoglutamyl form of this vitamin that is used commercially in supplements and in fortified foods.
How do you synthesize quinoxalines?
The classical synthesis of quinoxalines involves the condensation of an aromatic 1, 2-diamine with a 1, 2-dicarbonyl compound. The reaction is facile and is the most widely used synthetic method for both quinoxaline itself and its derivatives.
What is the role of quinoxaline derivatives in organic chemistry?
Also Quinoxaline derivatives constitute useful intermediates in organic synthesis. The pharmaco-logical importance of quinoxalines and their utility as building blocks in organic synthesis have directed considerable research activities toward the synthesis of suitably substituted quinoxaline rings.
How are quinoxalines produced from imides 182 and 183?
Another quinoxaline-yielding rearrangement, reported by Hanaineh-Abdelnour and coworkers, entailed treating imides 182 with sodium azide to produce quinoxalines 183 in moderate to good yields < 99H2931, 99T11859 >. The reaction presumably proceeds by a nitrene insertion to close the pyrazine ring.
What is quinoxaline made of?
Quinoxaline, also called a benzopyrazine, in organic chemistry, is a heterocyclic compound containing a ring complex made up of a benzene ring and a pyrazine ring and they are isomeric with cinnolenes, phthalazinesand quinazolines[2].